EP3456875B1 - Grained artificial leather - Google Patents

Grained artificial leather Download PDF

Info

Publication number
EP3456875B1
EP3456875B1 EP17796022.6A EP17796022A EP3456875B1 EP 3456875 B1 EP3456875 B1 EP 3456875B1 EP 17796022 A EP17796022 A EP 17796022A EP 3456875 B1 EP3456875 B1 EP 3456875B1
Authority
EP
European Patent Office
Prior art keywords
artificial leather
mass
grain
base material
flame retardant
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP17796022.6A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP3456875A1 (en
EP3456875A4 (en
Inventor
Kimio Nakayama
Naoto Narumoto
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kuraray Co Ltd
Original Assignee
Kuraray Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kuraray Co Ltd filed Critical Kuraray Co Ltd
Publication of EP3456875A1 publication Critical patent/EP3456875A1/en
Publication of EP3456875A4 publication Critical patent/EP3456875A4/en
Application granted granted Critical
Publication of EP3456875B1 publication Critical patent/EP3456875B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
    • D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
    • D06M13/285—Phosphines; Phosphine oxides; Phosphine sulfides; Phosphinic or phosphinous acids or derivatives thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/18—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with two layers of different macromolecular materials
    • D06N3/183—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with two layers of different macromolecular materials the layers are one next to the other
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/44—Oxides or hydroxides of elements of Groups 2 or 12 of the Periodic Table; Zincates; Cadmates
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
    • D06M11/45—Oxides or hydroxides of elements of Groups 3 or 13 of the Periodic Table; Aluminates
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/224—Esters of carboxylic acids; Esters of carbonic acid
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
    • D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
    • D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
    • D06M13/288—Phosphonic or phosphonous acids or derivatives thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
    • D06M23/08—Processes in which the treating agent is applied in powder or granular form
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0002—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0002—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate
    • D06N3/0004—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate using ultra-fine two-component fibres, e.g. island/sea, or ultra-fine one component fibres (< 1 denier)
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0002—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate
    • D06N3/0015—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate using fibres of specified chemical or physical nature, e.g. natural silk
    • D06N3/0036—Polyester fibres
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0056—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the compounding ingredients of the macro-molecular coating
    • D06N3/0063—Inorganic compounding ingredients, e.g. metals, carbon fibres, Na2CO3, metal layers; Post-treatment with inorganic compounds
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0056—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the compounding ingredients of the macro-molecular coating
    • D06N3/0068—Polymeric granules, particles or powder, e.g. core-shell particles, microcapsules
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/12—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
    • D06N3/14—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyurethanes
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N2209/00—Properties of the materials
    • D06N2209/06—Properties of the materials having thermal properties
    • D06N2209/067—Flame resistant, fire resistant
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N2211/00—Specially adapted uses
    • D06N2211/12—Decorative or sun protection articles
    • D06N2211/28—Artificial leather
    • D—TEXTILES; PAPER
    • D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
    • D10B2331/04—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyesters, e.g. polyethylene terephthalate [PET]

Definitions

  • the present invention relates to a grain-finished artificial leather having both a high level of flame retardancy and an excellent texture.
  • a grain-finished artificial leather in which a grain-like resin layer is stacked on an artificial leather base material obtained by impregnating an elastic polymer into a fiber-entangled body, such as a non-woven fabric, of ultrafine fibers.
  • the grain-finished artificial leather has been used as an alternative to a natural leather for the materials of shoes, clothing, gloves, bags, balls and the interior materials for buildings and vehicles.
  • Natural leather includes dense collagenous fibers, and thus has both suppleness and a high level of fullness (voluminousness). When natural leather is bent, such a high level of fullness allows the formation of fine luxurious fold creases with roundness, and also achieves elegant drape. However, it has been difficult to obtain a natural leather with stable quality. Since the collagenous fibers have low heat resistance and low water resistance, it has been difficult for natural leather to be used in applications for which heat resistance or high water resistance are required. To impart heat resistance or high water resistance to natural leather, a method is available in which a thick resin layer is formed on the surface of the leather. However, when a thick resin layer is formed, the suppleness of the natural leather would be lost.
  • the grain-finished artificial leather is superior to natural leather in quality stability, heat resistance, water resistance, and abrasion resistance, and is also easier to maintain.
  • voids that are not packed with an elastic polymer remain inside the fiber-entangled body of the grain-finished artificial leather, and, therefore, the grain-finished artificial leather is inferior to natural leather in fullness. Therefore, when bent, the grain-finished artificial leather does not bend with roundness as with the natural leather, and, instead, bends sharply as if in breaking. There is no luxurious quality to this kind of bending.
  • the number of voids is decreased by increasing the content ratio of the elastic polymer in the fiber-entangled body, the resilience of the elastic polymer increases, resulting in a rubber-like, rigid texture.
  • PTL 1 listed below discloses a grain-finished artificial leather with a high level of fullness that is obtained by stacking a grain-like resin layer on an artificial leather base material containing a filler, a liquid non-volatile oil, and an elastic polymer.
  • leather-like sheets such as artificial leather sheets and synthetic leather sheets have been used as the interior materials for public transports such as aircrafts, vessels, and railroad vehicles, and the interior materials for public buildings such as hotels and department stores.
  • the materials of interior materials that are used in public places are required have a high level of flame retardancy such as self-extinguishing properties, low smoke generation, and low heat generation in order to ensure safety in the event of a fire.
  • halogen-based flame retardants having high flame retardancy performance have hitherto been widely blended in the materials such as interior materials.
  • halogen-based flame retardants generate a toxic halogen gas when burned.
  • PTL 2 listed below discloses a fiber-urethane resin stack including, on at least one side of a fiber fabric, an adhesive layer made of a urethane resin containing a metal salt of dialkyl phosphinic acid, and a skin layer made of a urethane resin that is provided on the adhesive layer.
  • PTL 3 listed below discloses a synthetic leather including a base material layer made of a non-woven fabric or a knitted or woven fabric, an adhesive layer stacked on the base material layer, and a skin layer stacked on the adhesive layer, wherein 17 g/m 2 or more and 90 g/m 2 or less of a flame retardant is contained in the adhesive layer, and the glass transition temperature (Tg) of a resin forming the adhesive layer is -20°C or less.
  • PTL4 discloses a flame-retardant artificial leather having a sense of softness, fullness and flexibility. It comprises a substrate of entangled ultrafine fibers, a flame-retardant filler including dispersed solid microparticles and a liquid non-volatile oil.
  • a grain-finished artificial leather that uses an artificial leather base material obtained by impregnating an elastic polymer into voids inside a fiber-entangled body of ultrafine fibers is characterized by being superior in suppleness and fullness to a synthetic leather including a knitted or woven fabric of fibers of about 1 to 5 dtex, which are also called regular fibers, as the base material.
  • a fiber-entangled body of densely entangled ultrafine fibers has a significantly large surface area as compared with a knitted or woven fabric of regular fibers, and thus is flammable.
  • An elastic polymer that has been added into a grain-like resin layer or a fiber-entangled body is more flammable than the resin forming the fibers.
  • An aspect of the present invention is directed to a grain-finished artificial leather according to claim 1, including: an artificial leather base material; and a resin layer stacked on at least one surface of the artificial leather base material, wherein the artificial leather base material contains: a fiber-entangled body of ultrafine fibers; wherein the ultrafine fibers have an average fineness of 0.9 dtex or less; 3 to 50 mass% of a first elastic polymer; 2.5 to 6 mass%, in terms of phosphorus atoms, of first phosphorous-based flame retardant particles having an average particle size of 1 to 10 ⁇ m; and 1 to 6 mass% of a plasticizer wherein the artificial leather base material contains a fatty acid ester as the plasticizer, and the resin layer contains: a second elastic polymer; and a total content, in terms of phosphorus atoms or in terms of hydroxyl groups, of 0 to 8 mass% of flame retardant particles having an average particle size of 1 to 10 ⁇ m and being at least one selected from the group consisting of second phosphorous-based flame
  • the artificial leather base material contains 0.5 to 5 mass% of a fatty acid ester as the plasticizer, because a high level of flame retardancy and an excellent texture can be achieved. It is preferable that the artificial leather base material further contains a second metal hydroxide particles, because a high level of flame retardancy and an excellent texture can be achieved. It is preferable that a total content, in terms of phosphorus atoms or in terms of hydroxyl groups, of the first phosphorous-based flame retardant particles and the second metal hydroxide particles contained in the artificial leather base material is 2 to 6 mass%.
  • a total content, in terms of phosphorus atoms or in terms of hydroxyl groups, of the flame retardant particles contained in the resin layer is 2 to 8 mass%, because a higher level of flame retardancy can be achieved.
  • first phosphorous-based flame retardant particles or the second phosphorous-based flame retardant particles it is preferable to use a polyphosphate, an organic metal phosphate, an organic metal phosphinate, and an organic metal phosphonate.
  • first metal hydroxide particles or the second metal hydroxide particles it is preferable to use aluminum hydroxide and magnesium hydroxide.
  • the first elastic polymer contains 60 mass% or more of a polycarbonate-based polyurethane, and the polyurethane has a 100% modulus of 0.5 to 5 MPa, because of excellent mechanical properties.
  • the second elastic polymer contains 60 mass% or more of a polycarbonate-based polyurethane, because of excellent abrasion resistance.
  • the artificial leather base material contains polyester-based fibers as the ultrafine fibers, and has an apparent density of 0.60 to 0.85 g/cm 3 , because both fullness and a flexible texture, in particular, are provided.
  • a grain-finished artificial leather is a grain-finished artificial leather including an artificial leather base material, and a resin layer stacked on at least one surface of the artificial leather base material.
  • the artificial leather base material includes a fiber-entangled body of ultrafine fibers, wherein the ultrafine fibers have an average fineness of 0.9 dtex or less; 3 to 50 mass% of a first elastic polymer, 2.5 to 6 mass%, in terms of phosphorus atoms, of first phosphorous-based flame retardant particles having an average particle size of 1 to 10 ⁇ m, and 1 to 6 mass% of a plasticizer, wherein the artificial leather base material contains a fatty acid ester as plasticizer.
  • the resin layer contains a second elastic polymer, and a total content, in terms of phosphorus atoms or in terms of hydroxyl groups, of 0 to 8 mass% of flame-retardant particles having an average particle size of 1 to 10 ⁇ m and being at least one selected from the group consisting of second phosphorous-based flame retardant particles and first metal hydroxide particles.
  • a grain-finished artificial leather will be described in detail, in conjunction with an exemplary production method thereof.
  • the fiber-entangled body of ultrafine fibers examples include fiber structures such as a non-woven fabric, woven fabric, knitted fabric, of ultrafine fibers.
  • a non-woven fabric of ultrafine fibers is particularly preferable because it has a high fiber density and thus has low density unevenness and high homogeneity, thus providing an artificial leather base material having excellent suppleness and fullness.
  • a non-woven fabric of ultrafine fibers will be described in detail as a representative example of the fiber-entangled body of ultrafine fibers.
  • a non-woven fabric of ultrafine fibers is obtained, for example, by subjecting ultrafine fiber-generating fibers such as island-in-the-sea (matrix-domain) composite fibers to entangling treatment and then to ultrafine fiber-generating treatment.
  • ultrafine fiber-generating fibers such as island-in-the-sea (matrix-domain) composite fibers
  • matrix-domain composite fibers such as island-in-the-sea (matrix-domain) composite fibers
  • ultrafine fiber-generating fibers such as island-in-the-sea (matrix-domain) composite fibers
  • the present embodiment describes in detail a case where the island-in-the-sea composite fibers are used, it is possible to use ultrafine fiber-generating fibers other than the island-in-the-sea composite fibers, or to directly spin ultrafine fibers without using ultrafine fiber-generating fibers.
  • any fibers capable of forming ultrafine fibers may be used, including: for example, strip/division-type fibers in which a plurality of ultrafine fibers are lightly bonded immediately after spinning, and separated by a mechanical operation, to form a plurality of ultrafine fibers; and petal-shaped fibers obtained by alternately assembling a plurality of resins in a petal shape in a melt spinning process.
  • thermoplastic resin for forming a selectively-removable sea component (matrix component) of island-in-the-sea composite fibers and a thermoplastic resin for forming island components (domain components), i.e., resin components for forming ultrafine fibers, of the island-in-the-sea composite fibers are melt spun and then stretched, thereby obtaining island-in-the-sea composite fibers.
  • thermoplastic resin for the sea component a thermoplastic resin that differs from the resin for the island components in solubility in a solvent or in decomposability in a decomposition agent is selected.
  • thermoplastic resin forming the sea component include water-soluble polyvinyl alcohol-based resins, polyethylene, polypropylene, polystyrene, ethylene-propylene resins, ethylene-vinyl acetate resins, styrene-ethylene resins, and styrene-acrylic resins.
  • thermoplastic resin that defines the island components and that constitutes the resin component forming the ultrafine fibers
  • any resin capable of forming island-in-the-sea composite fibers and ultrafine fibers can be used.
  • aromatic polyesters such as polyethylene terephthalate (PET), isophthalic acid-modified PET, sulfoisophthalic acid-modified PET, polybutylene terephthalate, and polyhexamethylene terephthalate
  • aliphatic polyesters such as polylactic acid, polyethylene succinate, polybutylene succinate, polybutylene succinate adipate, and polyhydroxybutyrate-polyhydroxyvalerate resin
  • polyamides such as polyamide 6, polyamide 66, polyamide 10, polyamide 11, polyamide 12, and polyamide 6-12
  • polyolefins such as polypropylene, polyethylene, polybutene, polymethylpentene, and a chlorine-based polyolefin.
  • PET or modified PET polylactic acid, polyamide 6, polyamide 12, polyamide 6-12, polypropylene, are preferable.
  • PET and a modified resin such as isophthalic acid-modified PET are preferable because they have excellent shrinkability and can provide a high level of fullness.
  • the ratio of modification in the modified PET is preferably 0.1 to 30 mol%, more preferably 0.5 to 15 mol%, further preferably 1 to 10 mol%.
  • Examples of the production method of the non-woven fabric of ultrafine fibers include a method in which island-in-the-sea composite fibers are melt spun to produce a web, and the web is subjected to entangling treatment, and thereafter the sea component is selectively removed from the island-in-the-sea composite fibers, to form ultrafine fibers.
  • Examples of the production method of the web include a method in which filaments of the island-in-the-sea composite fibers that have been spun by spunbonding are collected on a net, without being cut, to form a filament web, and a method in which filaments are cut into staples to form a staple web.
  • a filament web is particularly preferable because of excellent denseness and fullness.
  • the formed web may be subjected to fusion bonding treatment in order to impart shape stability thereto.
  • fusion bonding treatment examples include a method in which about 5 to 100 layers of the web are placed on top of each other, and subjected to needle punching or high-pressure water jetting treatment.
  • a filament means a continuous fiber, rather than a staple that has been intentionally cut after being spun. More specifically, a filament means a fiber other than a staple that has been intentionally cut so as to have a fiber length of about 3 to 80 mm, for example.
  • the fiber length of the island-in-the-sea composite fibers before being subjected to ultrafine fiber generation is preferably 100 mm or more, and may have a fiber length of several meters, several hundred meters, several kilometers, or more, as long as the fibers are technically producible and are not inevitably cut during the production process. Note that some of filaments may be inevitably cut into staples during the production process by needle punching during entanglement or surface buffing.
  • fiber shrinking treatment such as heat shrinking treatment using water vapor may be performed, thus densifying the island-in-the-sea composite fibers to enhance the fullness.
  • the sea component of the island-in-the-sea composite fibers is removed by dissolution or decomposition at an appropriate stage after the web has been formed. Through such removal by decomposition or through dissolution and extraction, the island-in-the-sea composite fibers are subjected to ultrafine fiber generation, and ultrafine fibers in the form of fiber bundles are formed.
  • the average fineness of the ultrafine fibers is preferably 0.9 dtex or less, more preferably 0.001 to 0.9 dtex, particularly preferably 0.01 to 0.6 dtex, especially preferably 0.01 to 0.4 dtex.
  • the average fineness is excessively high, a non-woven fabric with insufficient denseness is obtained.
  • ultrafine fibers having an excessively low average fineness tend to have poor productivity, or the ultrafine fibers tend to bundle together and increases the rigidity of the non-woven fabric.
  • the average fineness a cross section of the artificial leather in the thicknesses direction is imaged using a scanning microscope with a magnification of 2000X, to obtain a cross-sectional area of single fibers, and the fineness of a single fiber can be calculated from the cross-sectional area and the specific gravity of the resin that forms the fibers.
  • the average fineness can be defined as an average value of the fineness of average 100 single fibers, evenly obtained from the captured image.
  • the thus obtained non-woven fabric of ultrafine fibers are subjected to thickness adjustment and planarization treatment, if necessary. Specifically, slicing treatment or buffing treatment is performed.
  • a non-woven fabric that is a fiber-entangled body of ultrafine fibers is obtained.
  • the thickness of the fiber-entangled body is preferably about 100 to 3000 ⁇ m, more preferably about 300 to 2000 ⁇ m.
  • the apparent density of the fiber-entangled body is preferably about 0.60 to 0.80 g/cm 3 , more preferably about 0.65 to 0.75 g/cm 3 , because an artificial leather base material having both fullness and a flexible texture can be obtained.
  • the artificial leather base material of the present embodiment further includes 3 to 50 mass% of a first elastic polymer, 2.5 to 6 mass%, in terms of phosphorus atoms, of first phosphorous-based flame retardant particles having an average particle size of 1 to 10 ⁇ m, and 1 to 6 mass% of a plasticizer. These are added into the fiber-entangled body of ultrafine fibers.
  • the first elastic polymer, the first phosphorous-based flame retardant particles, and the plasticizer that are to be added into the fiber-entangled body may be simultaneously added as a mixture thereof to the fiber-entangled body, or each may be added in separate processes. Alternatively, one of these components may be added into the fiber-entangled body, and, thereafter, a mixture of the other two components may be added.
  • the first elastic polymer is added into the fiber-entangled body in order to impart rigidity and shape stability or suppleness and a high level of fullness to the artificial leather base material by restraining the ultrafine fibers.
  • the first elastic polymer is added, for example, by a method in which an aqueous liquid such as an emulsion of an elastic polymer such as polyurethane is impregnated into a fiber-entangled body of ultrafine fiber-generating fibers before subjecting ultrafine fiber-generating fibers to ultrafine fiber generation, or a fiber-entangled body of ultrafine fibers after subjecting ultrafine fiber-generating fibers to ultrafine fiber generation, followed by solidification.
  • an aqueous liquid such as an emulsion of an elastic polymer is preferable because of the low environmental load.
  • Examples of the methods for impregnating an aqueous liquid of an elastic polymer into a fiber-entangled body of ultrafine fiber-generating fibers or a fiber-entangled body of ultrafine fibers include methods using a knife coater, a bar coater, or a roll coater, and a method involving dipping.
  • the elastic polymer can be agglomerated by a method in which heat treatment is performed in a drying device at 50 to 200°C, a method in which heat treatment is performed in a dryer after infrared heating, a method in which heat treatment is performed in a dryer after steam treatment, a method in which heat treatment is performed in a dryer after ultrasonic heating, or a combination of these methods.
  • elastic polymers such as rubbers and elastomers may be used.
  • the elastic polymers include diene-based rubbers (e.g., a butadiene rubber, an isoprene rubber, a chloroprene rubber, and a styrene-butadiene rubber), nitrile-based rubbers (e.g., a nitrile rubber and a hydrogenated nitrile rubber), acryl-based rubbers (e.g., an acrylic rubber), urethane-based rubbers (e.g., a polyether urethane rubber and a polyester urethane rubber), silicone rubbers, olefin-based rubbers (e.g., an ethylene-propylene rubber), fluorine rubbers, polystyrene-based elastomers (e.g., a styrene-butadiene block copolymer, a styrene-isoprene block cop
  • polyurethane examples include various polyurethanes obtained by reacting a polymer polyol having an average molecular weight of 200 to 6000, an organic polyisocyanate, and a chain extender at a predetermined molar ratio.
  • polymer polyol examples include polyether-based polyols such as polyethylene glycol, polypropylene glycol, polytetramethylene glycol, and poly(methyl tetramethylene glycol), and copolymers thereof; polyester-based polyols such as polybutylene adipate diol, polybutylene sebacate diol, polyhexamethylene adipate diol, poly(3-methyl-1,5-pentylene adipate)diol, poly(3-methyl-1,5-pentylene sebacate)diol, and polycaprolactone diol, and copolymers thereof; polycarbonate-based polyols such as polyhexamethylene carbonate diol, poly(3-methyl-1,5-pentylene carbonate)diol, polypentamethylene carbonate diol, and polytetramethylene carbonate diol, and copolymers thereof; and polyester carbonate polyol.
  • a multifunctional alcohol such as a trifunctional alcohol or a tetrafunctional alcohol, or a short-chain alcohol such as ethylene glycol may also be used. These may be used alone or in a combination of two or more.
  • amorphous polycarbonate-based polyols, alicyclic polycarbonate-based polyols, linear polycarbonate-based polyol copolymers, polyether-based polyols are preferable because an artificial leather base material with well-balanced flexibility and fullness can be obtained.
  • organic polyisocyanate examples include non-yellowing diisocyanates, including, aliphatic or alicyclic diisocyanates such as hexamethylene diisocyanate, isophorone diisocyanate, norbornene diisocyanate, and 4,4'-dicyclohexyl methane diisocyanate; and aromatic diisocyanates such as 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, 4,4'-diphenyl methane diisocyanate, and xylylene diisocyanate polyurethane.
  • a multifunctional isocyanate such as trifunctional isocyanate or tetrafunctional isocyanate may also be used.
  • 4,4'-dicyclohexyl methane diisocyanate, isophorone diisocyanate, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, 4,4'-diphenyl methane diisocyanate, and xylylene diisocyanate are preferable because of their excellent mechanical properties.
  • chain extender examples include diamines such as hydrazine, ethylene diamine, propylene diamine, hexamethylene diamine, nonamethylene diamine, xylylene diamine, isophorone diamine, piperazine and derivatives thereof, adipic acid dihydrazide, and isophthalic acid dihydrazide; triamines such as diethylenetriamine; tetramines such as triethylene tetramine; diols such as ethylene glycol, propylene glycol, 1,4-butane diol, 1,6-hexane diol, 1,4-bis( ⁇ -hydroxyethoxy)benzene, and 1,4-cyclohexane diol; triols such as trimethylol propane; pentaols such as pentaerythritol; amino alcohols such as amino ethyl alcohol and amino propyl alcohol.
  • diamines such as hydrazine, ethylene diamine, propylene diamine,
  • hydrazine such as ethylamine, propylamine, and butylamine
  • carboxyl group-containing monoamine compounds such as 4-amino butanoic acid and 6-amino hexanoic acid
  • monools such as methanol, ethanol, propanol, and butanol may be used together with the chain extender during a chain extending reaction.
  • a crosslinked structure may be formed by adding a crosslinking agent containing, in the molecule, two or more functional groups capable of reacting with a functional group included in monomer units that form the polyurethane, such as a carbodiimide-based compound, an epoxy-based compound, an oxazoline-based compound, or a self-crosslinking compound such as a polyisocyanate-based compound and a multifunctional block isocyanate compound.
  • a crosslinking agent containing, in the molecule, two or more functional groups capable of reacting with a functional group included in monomer units that form the polyurethane, such as a carbodiimide-based compound, an epoxy-based compound, an oxazoline-based compound, or a self-crosslinking compound such as a polyisocyanate-based compound and a multifunctional block isocyanate compound.
  • Examples of the emulsion of the polyurethane include a forcedly emulsified polyurethane emulsion that does not include any ionic group in the polyurethane skeleton and has been emulsified by adding an emulsifier; a self-emulsified polyurethane emulsion that includes an ionic group such as a carboxyl group, a sulfonic acid group, and an ammonium group in the polyurethane skeleton and that has been emulsified by self-emulsification; and a polyurethane emulsion that uses an emulsifier and an ionic group in the polyurethane skeleton in combination.
  • a forcedly emulsified polyurethane emulsion that does not include any ionic group in the polyurethane skeleton and has been emulsified by adding an emulsifier
  • a self-emulsified polyurethane emulsion that includes an ionic
  • Examples of the method for introducing a carboxyl group into the polyurethane skeleton include a method in which units of carboxyl group-containing diols such as 2,2-bis(hydroxymethyl)propionic acid, 2,2-bis(hydroxymethyl)butanoic acid, and 2,2-bis(hydroxymethyl)valeric acid are incorporated into the polyurethane skeleton.
  • a polyurethane emulsion including 20 to 100 mass% of a forcedly emulsified polyurethane and 0 to 80 mass% of a self-emulsified polyurethane, in particular, including 30 to 100 mass% of a forcedly emulsified polyurethane and 0 to 70 mass% of a self-emulsified polyurethane, because a flexible texture can be achieved.
  • the average dispersed particle size of the emulsion of the polyurethane is preferably 0.01 to 1 ⁇ m, more preferably 0.03 to 0.5 ⁇ m.
  • the polyurethane has a 100% modulus of preferably 0.5 to 5 MPa, more preferably 1 to 4 MPa, because a flexible texture can be achieved by a combined use with the plasticizer.
  • the 100% modulus When the 100% modulus is excessively low, the polyurethane tends to be softened when subjected to heat, and thus restrains the ultrafine fibers, resulting in a reduction in the flexible texture.
  • the 100% modulus When the 100% modulus is excessively high, the polyurethane tends to be hardened. It is preferable that polycarbonate-based polyurethane constitutes 60 mass% or more of the polyurethane because of excellent durability.
  • the ratio of the first elastic polymer contained in the artificial leather base material is 3 to 50 mass%, preferably 5 to 45 mass%, more preferably 8 to 30 mass%.
  • the content ratio of the first elastic polymer is less than 3 mass%, the fullness and the shape stability are reduced.
  • the content ratio exceeds 50 mass%, the rubber-like feel is increased, thus compromising the texture and reducing the flame retardancy.
  • the emulsion When an emulsion of an elastic polymer is impregnated into a fiber-entangled body of ultrafine fiber-generating fibers or a fiber-entangled body of ultrafine fibers, and thereafter dried, the emulsion may migrate to the surface layer of the fiber-entangled body of ultrafine fiber-generating fibers or the fiber-entangled body of ultrafine fibers, and thus may not be uniformly added in the thickness direction.
  • the migration can be suppressed by, for example, adjusting the particle size of the elastic polymer in the emulsion; adjusting the type and the amount of the ionic groups of the elastic polymer; reducing the water dispersion stability by addition of an ammonium salt that undergoes a pH change at a temperature of about 40 to 100°C; or reducing the water dispersion stability at about 40 to 100°C by addition of a monovalent or divalent alkali metal salt or alkaline-earth metal salt, a nonionic emulsifier, an associative water-soluble thickener, an associative heat-sensitive gelling agent such as a water-soluble silicone-based compound, or a water-soluble polyurethane-based compound.
  • the emulsion may be allowed to migrate such that the elastic polymer is unevenly distributed on the surface.
  • the elastic polymer may be present preferentially on the surface side by changing the conditions for the drying method or the addition method between the surface side and the back side.
  • the first elastic polymer may be impregnated inside the fiber bundles, or may be attached to the outside of the fiber bundles.
  • the texture can be adjusted as appropriate by changing the degree of restraint of the ultrafine fibers forming the fiber bundles.
  • the water-soluble thermoplastic resin is removed from the island-in-the-sea composite fibers, to form voids inside the ultrafine fiber bundles.
  • the first phosphorous-based flame retardant particles are a component that imparts, to the artificial leather base material, flame retardancy that achieves good self-extinguishing properties, as well as a low burn heat value and a low smoke density without generating a toxic gas during burning, and a texture with fullness.
  • First phosphorous-based flame retardant particles having an average particle size of 1 to 10 ⁇ m achieve a synergistic effect with the plasticizer, thus imparting a high level of flame retardancy and a flexible texture with fullness to the artificial leather base material.
  • the first phosphorous-based flame retardant particles in the present embodiment are a phosphorus atom-containing compound that is a particulate solid at room temperature.
  • a phosphorus atom-containing compound that is a particulate solid at room temperature.
  • Specific examples thereof include polyphosphates such as melamine polyphosphate, melam polyphosphate, melem polyphosphate, and ammonium polyphosphate; organic metal phosphates, organic metal phosphinates such as metal dialkyl phosphinates, and organic metal phosphonates. These may be used alone or in a combination of two or more.
  • metal dialkyl phosphinates, polyphosphates, and ammonium polyphosphate that has been encapsulated by melamine are preferable because of a high level of flame retardance effect achieved by good water resistance, good heat resistance, and a high phosphorus atom content.
  • the first phosphorous-based flame retardant particles have low water-solubility, and the solubility is preferably 1% or less, because changes under a humidified atmosphere during use or in a wetted state do not occur.
  • the melting point and the decomposition temperature are preferably 250°C or more, more preferably 300°C or more, because changes under a high-atmosphere during use do not occur.
  • the average particle size of the first phosphorous-based flame retardant particles is 1 to 10 ⁇ m, preferably 2 to 7 ⁇ m.
  • the average particle size is less than 1 ⁇ m, the texture of the artificial leather base material is hardened.
  • the average particle size exceeds 10 ⁇ m, it becomes difficult for the particles to be uniformly added into the voids of the fiber-entangled body, resulting in a reduction in the flame retardancy.
  • the ratio of the first phosphorous-based flame retardant particles included in the artificial leather base material, in terms of phosphorus atoms, is 2.5 to 6 mass%, preferably 3.5 to 5.5 mass%.
  • the content of the first phosphorous-based flame retardant particles is less than 2.5 mass% in terms of phosphorus atoms, a high level of flame retardancy cannot be achieved.
  • the content of the first phosphorous-based flame retardant particles exceeds 6 mass% in terms of phosphorus atoms, the suppleness is lost.
  • the artificial leather base material may further contain metal hydroxide particles (second metal hydroxide particles).
  • the second metal hydroxide particles impart, to the artificial leather base material, flame retardancy that achieves good self-extinguishing properties, as well as a low burn heat value and a low smoke density without generating a toxic gas during burning, and a texture with fullness.
  • the second metal hydroxide particles also achieve a synergistic effect with the plasticizer, thus imparting a high level of flame retardancy and a flexible texture with fullness to the artificial leather base material.
  • the second metal hydroxide particles are a metal compound that includes a hydroxyl group and is a particulate solid at room temperature, and specific examples thereof include aluminum hydroxide and magnesium hydroxide.
  • the average particle size of the second metal hydroxide particles is preferably 1 to 10 ⁇ m, more preferably 2 to 8 ⁇ m.
  • a total content, in terms of phosphorus atoms or in terms of hydroxyl groups, of the first phosphorous-based flame retardant particles and the second metal hydroxide particles is preferably 2 to 6 mass%, more preferably 2.5 to 6 mass%, particularly preferably 3.5 to 5.5 mass%.
  • the plasticizer is a component that imparts a texture having both suppleness and fullness to the artificial leather base material by suppressing reduction in the suppleness in the case of adding the first phosphorous-based flame retardant particles, and optionally the second metal hydroxide particles, to the fiber-entangled body.
  • the plasticizer in the present embodiment is a liquid, viscous, wax-like, or solid oil or fatty ester that is blended in order to soften the fibers, the elastic polymer, the flame retardant particles that constitute the artificial leather base material, and to enhance the plastic deformability of the constituting fibers, elastic polymer, and flame retardant particles.
  • fatty acid esters include fatty acid esters, hydrocarbon-based oils such as paraffin oil, hydrocarbon-based waxes, carnauba waxes, phthalic acid esters, phosphoric acid esters, and hydroxy carboxylic acid esters. These may be used alone or in a combination of two or more. Among these, fatty acid esters are preferable in that they impart a texture having both suppleness and fullness to the artificial leather base material, and do not reduce the flame retardancy and the durability, when used in combination with the first phosphorous-based flame retardant particles, and the optionally added second metal hydroxide particles and elastic polymer.
  • hydrocarbon-based oils such as paraffin oil, hydrocarbon-based waxes, carnauba waxes, phthalic acid esters, phosphoric acid esters, and hydroxy carboxylic acid esters. These may be used alone or in a combination of two or more.
  • fatty acid esters are preferable in that they impart a texture having both suppleness and fullness to the
  • fatty acid esters examples include compounds obtained by esterification of an alcohol component and an acid component, such as monohydric alcohol esters, monohydric alcohol esters of polybasic acids, fatty acid esters of polyhydric alcohols and derivatives thereof, and fatty acid esters of glycerin.
  • the alcohol component examples include methyl alcohol, isopropyl alcohol, n-butyl alcohol, isobutyl alcohol, n-octyl alcohol, 2-ethylhexyl alcohol, n-decyl alcohol, isodecyl alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, octyl dodecyl alcohol, glycerin, sorbitan, polyoxyethylene sorbitan, polyoxyethylene sorbitol, ethylene glycol, polyethylene glycol, propylene glycol, pentaerythritol, and polyoxyethylene bisphenol A.
  • the acid component examples include caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, behenic acid, cocconut fatty acid, methacrylic acid, 2-ethylhexanoic acid, adipic acid, azelaic acid, maleic acid, and sebacic acid.
  • fatty acid esters include cetyl 2-ethylhexanoate, cocconut fatty acid methyl, methyl laurate, isopropyl myristate, isopropyl palmitate, 2-ethylhexyl palmitate, octyldodecyl myristate, methyl stearate, butyl stearate, 2-ethylhexyl stearate, isotridecyl stearate, methyl oleate, myristyl myristate, stearyl stearate, isobutyl oleate, diisobutyl adipate, diisodecyl adipate, sorbitan monolaurate, sorbitan monopalmitate, sorbitan monostearate, sorbitan tristearate, sorbitan monooleate, sorbitan trioleate, sorbitan monostearate, sorbitan sesquio
  • the fatty acid ester may be used in the form of a dispersion in which a fatty acid ester is dispersed in a dispersing medium such as a water or a liquid mixture of water and a polar solvent such as alcohol.
  • a fatty acid ester having a melting point of about 60°C or less and preferably being a liquid compound at room temperature because it can impart a texture having both suppleness and fullness to the artificial leather base material, and does not reduce the flame retardancy or the durability, when used in combination with phosphorous-based flame retardant particles and metal hydroxide.
  • a fatty acid ester of a fatty acid having a 12 to 18 carbon atoms and polyhydric alcohol because it can achieve a more flexible texture and fullness even when phosphorous-based flame retardant particles are added.
  • the ratio of the plasticizer included in the artificial leather base material is 1 to 6 mass%, preferably 2 to 5 mass%.
  • the content of the plasticizer is less than 1 mass%, the loss of the suppleness caused by addition of the first phosphorous-based flame retardant particles and the optionally added second metal hydroxide particles cannot be sufficiently inhibited.
  • the content exceeds 6 mass%, the plasticizer tends to reduce the flame retardancy, and to bleed out, thus causing stickiness or the like.
  • a fatty acid ester is included as the plasticizer, 0.5 to 5 mass%, preferably 1 to 3 mass% of the fatty acid ester is contained
  • the first phosphorous-based flame retardant particles, and optionally the second metal hydroxide particles and the plasticizer are added to the fiber-entangled body.
  • Specific examples thereof include a method in which a dispersion containing the first phosphorous-based flame retardant particles, and optionally the second metal hydroxide particles and the plasticizer, is impregnated into a fiber-entangled body by dip-nipping, followed by drying.
  • the viscosity of the dispersion to be impregnated is within the range that allows the dispersion to be impregnated into the fiber-entangled body.
  • the solution viscosity as measured by a rotational viscometer is preferably about 10 to 1000 MPa ⁇ s (millipascal-second), more preferably about 50 to 500 MPa ⁇ s.
  • the volatile components in the dispersion such as a dispersing medium, are dried, and the first phosphorous-based flame retardant particles, and optionally the second metal hydroxide particles and the plasticizer, remain in the voids between the fibers of the fiber-entangled body.
  • drying conditions include conditions that the fiber-entangled body is dried at 70 to 150°C for about 1 to 10 minutes.
  • an artificial leather base material in which the elastic polymer, the first phosphorous-based flame retardant particles, and optionally the second metal hydroxide particles and the plasticizer, are impregnated into a fiber-entangled body is obtained.
  • the artificial leather base material may be optionally subjected to: thickness adjustment and planarization treatment by slicing treatment or buffing treatment; or finishing treatment such as flexibilizing treatment by crumpling, softening treatment by milling, reverse seal brushing treatment, antifouling treatment, hydrophilization treatment, lubricant treatment, softener treatment, antioxidant treatment, ultraviolet absorber treatment, fluorescent agent treatment, and flame retardant treatment.
  • the method for softening processing is preferable to use a method in which the artificial leather base material is brought into close contact with an elastic sheet, and mechanically shrunk in a vertical direction (MD on production line), and then subjected to heat treatment in the shrunk state for heat setting.
  • the artificial leather base material can be softened, while the smoothness of its surface is enhanced.
  • the thickness of the thus obtained artificial leather base material is preferably about 100 to 3000 ⁇ m, more preferably about 300 to 2000 ⁇ m.
  • the apparent density of the artificial leather base material is preferably 0.55 to 0.85 g/cm 3 , more preferably 0.60 to 0.80 g/cm 3 , because of well-balanced fullness and a flexible texture.
  • the grain-finished artificial leather of the present embodiment can be obtained by forming a grain-like resin layer on the artificial leather base material.
  • the resin layer may be a single layer, or may have a stacked structure composed of a plurality of layers, including, for example, a skin layer and an adhesive layer. Note that when the resin layer has a stacked structure composed of a plurality of layers, the entire stacked structure is formed as a resin layer.
  • the resin layer of the present embodiment contains a second elastic polymer, and a total content, in terms of phosphorus atoms or in terms of hydroxyl groups, of 8 mass% or less of flame retardant particles having an average particle size of 1 to 10 ⁇ m and being selected from the group consisting of second phosphorous-based flame retardant particles and first metal hydroxide particles.
  • the second elastic polymer is an elastic polymer included in the resin layer.
  • the second elastic polymer include polyurethanes, acryl-based elastic bodies, silicone-based elastic bodies, diene-based elastic bodies, nitrile-based elastic bodies, fluorine-based elastic bodies, polystyrene-based elastic bodies, polyolefin-based elastic bodies, polyamide-based elastic bodies, and halogen-based elastic bodies. These may be used alone or in a combination of two or more.
  • the layers of the stacked structure may include different types of elastic polymers. Among these, polyurethanes are preferable because of their excellent abrasion resistance and mechanical properties.
  • the second elastic polymer may contain a colorant, an ultraviolet absorber, a surfactant, another flame retardant, an antioxidant, , so long as the effects of the present invention are not impaired.
  • the second phosphorous-based flame retardant particles are a component that imparts, to the resin layer, a high level of flame retardancy that achieves good self-extinguishing properties, as well as a low burn heat value and a low smoke density without generating a toxic gas during burning, and the same materials as those included in the above-described artificial leather base material can be used.
  • the problem of the stickiness caused by bleeding-out on the surface during use as in the case of blending a liquid phosphorous-based flame retardant is less likely to occur.
  • the second phosphorous-based flame retardant particles preferably have low water-solubility, and the solubility is preferably 1% or less, because changes under a humidified atmosphere during use or in a wetted state do not occur.
  • the melting point and the decomposition temperature are preferably 250°C or more, more preferably 300°C or more, because changes are less likely to occur during use under a high-temperature atmosphere.
  • the average particle size of the second phosphorous-based flame retardant particles is 1 to 10 ⁇ m, preferably 2 to 7 ⁇ m.
  • the average particle size is less than 1 ⁇ m, it becomes more difficult for the particles to be uniformly dispersed in the resin layer, resulting in a reduction in the flame retardancy.
  • the average particle size exceeds 10 ⁇ m, the surface properties and the bendability tend to be reduced, and the flame retardancy tends to be reduced.
  • the first metal hydroxide particles are a hydroxyl group-containing metal compound that is a particulate solid at room temperature, and specific examples thereof include particles of aluminum hydroxide, magnesium hydroxide.
  • a polyurethane as the second elastic polymer, it is particularly preferable to use aluminum hydroxide because of its high flame retardance effect.
  • the average particle size of the second phosphorous-based flame retardant particles or the first metal hydroxide particles is 1 to 10 ⁇ m, preferably 2 to 8 ⁇ m.
  • the average particle size is less than 1 ⁇ m, the flame retardant particles are agglomerated and thus become difficult to be uniformly dispersed, as a result of which the flame retardancy is reduced.
  • the average particle size exceeds 10 ⁇ m, the surface area of the flame retardant is decreased, so that the flame retardancy is reduced, and the mechanical properties of the resin layer are also reduced.
  • the average particle size of the second phosphorous-based flame retardant particles or the first metal hydroxide can be measured by a known method such as a method using a refractive index.
  • a cross section of the artificial leather in the thickness direction or a cross section of the grain layer is imaged using a scanning microscope with a magnification of 1000X, and the number-average value of the diameters of average 100 flame retardant particles, evenly obtained from the captured image, is defined as the average particle size.
  • the total content of the flame retardant particles contained in the resin layer is 0 to 8 mass%, preferably 2 to 8 mass%, in terms of phosphorus atom and in terms of hydroxyl groups.
  • the resin layer is hardened, and is likely to form coarse grain and deep creases when bent.
  • the physical properties such as bendability, tear strength, surface abrasion tend to be reduced.
  • the method for forming the resin layer on the artificial leather base material include specifically dry forming or direct coating for example.
  • the dry forming is a method in which a coating liquid including a colored resin for forming a grain-like skin layer is applied to a release sheet as the resin layer, followed by drying to form a film, and then the film is attached to the surface of the artificial leather base material via an adhesive layer, followed by releasing the release sheet.
  • the direct coating is a method in which a coating liquid for forming the resin layer is directly applied to the surface of the artificial leather base material using a roll coater or a spray coater, followed by drying.
  • a grain pattern may be formed on the resin layer by emboss processing.
  • Examples of the emboss processing include a method in which a skin layer is formed on a grained release paper having a grain pattern provided on its surface, and a method in which a grain pattern is transferred to the skin layer in an uncured state, followed by curing.
  • the thickness of the resin layer is preferably 10 to 1000 ⁇ m, more preferably 30 to 300 ⁇ m.
  • the grain-finished artificial leather of the present embodiment is obtained.
  • the apparent density of the grain-finished artificial leather of the present embodiment is preferably 0.60 to 0.85 g/cm 3 , more preferably 0.65 to 0.80 g/cm 3 , because a high level of fullness can be achieved.
  • the grain-finished artificial leather of the present embodiment has both suppleness and a high level of fullness that resemble those of natural leather.
  • the bending resistance of the grain-finished artificial leather as measured by a softness tester is preferably 3.5 mm or more, more preferably 4.0 mm or more for a thickness of 0.5 mm, and is preferably 3.0 mm or more for a thickness of 0.7 mm, and is preferably 2.5 mm or more for a thickness of 1 mm.
  • the grain-finished artificial leather of the present embodiment has a high level of flame retardancy, a flexible texture, and fullness, and therefore can be preferably used in applications for which a high level of flame retardancy, such as self-extinguishing properties, low smoke generation, and low heat generation, is required, including, for example, the interior furnishing of public transports such as aircrafts, vessels, and railroad vehicles, or the materials of seats or sofas and the interior furnishing such as walls in public buildings such as hotels and department stores.
  • a high level of flame retardancy such as self-extinguishing properties, low smoke generation, and low heat generation
  • molten resin was fed to a plurality of spinnerets for spinning set to a spinneret temperature of 260°C and having nozzle holes arranged in parallel, the nozzle holes being capable of forming a sectional surface on which 25 island components with a uniform sectional surface area distributed in a sea component, and the molten resin was discharged from the nozzle holes.
  • the discharged molten fibers were stretched by suction using a suction apparatus so as to provide an average spinning speed of 3700 m/min, and thereby to spin filaments of the island-in-the-sea composite fibers with a fineness of 3.3 dtex.
  • the spun filaments of the island-in-the-sea composite fibers were continuously piled on a movable net, and then lightly pressed with a metal roll at 42°C, to suppress the fuzzing on the surface.
  • the filaments of the island-in-the-sea composite fibers were removed from the net, and allowed to pass between a grid-patterned metal roll having a surface temperature of 55°C and a back roll.
  • the filaments were hot-pressed with a linear load of 200 N/mm, to obtain a filament web having a basis weight of 31 g/m 2 .
  • the web was needle-punched at a density of 3300 punch/cm 2 alternately from both sides by using 6-barb needles with a distance of 3.2 mm from the needle tip to the first barb at a punching depth of 8.3 mm.
  • the area shrinkage due to this needle punching treatment was 70%, and the basis weight of the entangled web after the needle punching was 460 g/m 2 .
  • the entangled web was allowed to pass for 30 seconds under a humidity of 50% RH at 70 °C at a take-up line speed of 10 m/min, to cause heat-moisture shrinking.
  • the area shrinkage before and after the heat-moisture shrinking treatment was 47%.
  • a forcedly emulsified amorphous polycarbonate-based polyurethane having a 100% modulus of 2.5 MPa and a self-emulsified amorphous polycarbonate urethane having a 100% modulus of 3.0 MPa were mixed at a ratio of 60/40 based on polyurethane solids, and an aqueous dispersion including 1.5 mass% of ammonium sulfate was further impregnated into the entangled non-woven fabric, followed by drying at 150°C.
  • PVA was removed by dissolution by repeatedly performing dip-nipping treatment in hot water at 95°C, thereby to produce a fiber-entangled body intermediate including a non-woven fabric in which fiber bundles each including 25 ultrafine filaments with a fineness of 0.1 dtex were entangled three-dimensionally.
  • the polyurethane content in the fiber-entangled body intermediate was 10 mass%.
  • the fiber-entangled body intermediate was sliced into two in the thickness direction, and buffed, and thereby finished into a fiber-entangled body with a thickness of approximately 0.5 mm.
  • the thus obtained fiber-entangled body had a thickness of 0.48 mm, a basis weight of 280 g/m 2 , and an apparent density of 0.56 g/cm 3 .
  • aqueous dispersion containing 22 mass% of aluminum dialkylphosphinate with an average particle size of 4 ⁇ m, 2.2 mass% of fatty acid ester as a plasticizer, and 2.2 mass% of paraffin oil was prepared. Then, the aqueous dispersion was impregnated into the fiber-entangled body at a pick-up rate of 90% relative to the non-woven fabric of ultrafine fibers, followed by drying of moisture at 120°C.
  • the fiber-entangled body was shrunk by 5.0% in a vertical direction (length-wise direction) by using a shrinkage processing apparatus (sanforizing machine manufactured by Komatsubara Tekko K.K.) for treatment at a drum temperature of 120°C in its shrinking portion, a drum temperature of 120°C in its heat setting portion, and a transport speed of 10 m/min, thereby to obtain an artificial leather base material.
  • the obtained artificial leather base material had a thickness of 0.50 mmm, a basis weight of 325 g/m 2 , and an apparent density of 0.65 g/cm 3 .
  • the artificial leather base material contained its components at the following proportion: 8.2 mass% of the elastic polymer, 17 mass% (3.9 mass% in terms of phosphorus atoms) of the aluminum dialkylphosphinate, 1.7 mass% of the fatty acid ester, and 1.7 mass% of the paraffin oil.
  • a polycarbonate-based polyurethane solution (Crisvon S-121, solid content: 30 mass%, manufactured by DIC Corporation) containing a pigment was applied onto a surface of a grained release sheet having a pattern of projections and recesses, followed by drying, thereby to form a grain layer film with a thickness of 30 ⁇ m.
  • the grain layer film formed on the grained release sheet was attached to the artificial leather base material.
  • the polyurethane adhesive layer thus formed had a thickness of 60 ⁇ m.
  • the resin layer in which the grain layer and the adhesive layer were attached to each other contained 3.4 mass% of the aluminum dialkylphosphinate in terms of phosphorus atoms and 0.43 mass% of the aluminum hydroxide in terms of hydroxyl groups, and the total content in terms of phosphorus atoms and in terms of hydroxyl groups was 3.8 mass%.
  • the obtained grain-finished artificial leather was evaluated according to the following evaluation methods.
  • the bending resistance was measured using a softness tester (leather softness measuring instrument ST 300, manufactured by MSA Engineering Systems Limited of the United Kingdom). Specifically, a predetermined ring with a diameter of 25 mm was set on a lower holder of the instrument, and thereafter, the grain-finished artificial leather was set on the lower holder.
  • a softness tester leather softness measuring instrument ST 300, manufactured by MSA Engineering Systems Limited of the United Kingdom. Specifically, a predetermined ring with a diameter of 25 mm was set on a lower holder of the instrument, and thereafter, the grain-finished artificial leather was set on the lower holder.
  • the grain-finished artificial leather was cut to a size of 20 x 20 cm, to prepare a sample. Then, the appearance of the leather when it was bent inward at the center thereof, and the appearance of the leather when it was held, were evaluated according to the following criteria.
  • the artificial leather had a rubber-like texture, strong resiliency, and also poor drape.
  • the artificial leather had a texture with a significantly low level of fullness, and formed coarse grain and deep creases when bent.
  • the test piece was heated/burned for 10 minutes using the burner flame and a heater with 25 kW/m 2 , and the smoke density Ds was measured 4 minutes thereafter.
  • the test piece was heated/burned for 10 minutes using a heater with 50 kW/m 2 , and the gross heat value and the peak heat value were measured 2 minutes thereafter.
  • the thickness (mm) and the basis weight (g/cm 2 ) were measured, and an apparent density (g/cm 3 ) was calculated from these values.
  • Grain-finished artificial leathers were obtained in the same manner as in Example 1, except that the compositions of the components in Example 1 were changed as shown in Table 1, and the obtained artificial leathers were evaluated. The results are shown in Table 1.
  • Grain-finished artificial leathers were obtained in the same manner as in Example 1, except that, as shown in Table 1, the fineness of the ultrafine fibers was changed to 0.9 dtex or 0.001 dtex, and aluminum hydroxide was contained as second metal hydroxide particles in the artificial leather base material, and a fatty acid ester and a phosphoric acid ester were used as the plasticizer contained in the artificial leather base material, and the obtained artificial leathers were evaluated. The results are shown in Table 1.
  • a grain-finished artificial leather was obtained in the same manner as in Example 1, except that the content of the first elastic polymer in the artificial leather base material was changed to 1 mass% by changing the concentration of the dispersion of the elastic polymer to 2.5 mass%, and the obtained artificial leather was evaluated. The results are shown in Table 2.
  • a grain-finished artificial leather was obtained in the same manner as in Example 1, except that the content of the first elastic polymer in the artificial leather base material was changed to 55 mass% by changing the concentration of the dispersion of the elastic polymer to 50 mass%, and the obtained artificial leather was evaluated. The results are shown in Table 2.
  • An artificial leather base material was obtained in the same manner as in Example 1, except that the impregnation and the drying were performed with the particle size of the first phosphorous-based flame retardant particles changed to 15 ⁇ m. Further, a grain-finished artificial leather was obtained in the same manner as in Example 1, except that the second phosphorous-based flame retardant particles and the first metal hydroxide blended in the resin layer each had an average particle size of 15 ⁇ m, and the obtained artificial leather was evaluated. The results are shown in Table 2.
  • a grain-finished artificial leather was obtained in the same manner as in Example 1, except that the impregnation and the drying were performed with the solid content of the first phosphorous-based flame retardant particles changed to 12 mass%, to change the content of the first phosphorous-based flame retardant particles to 2.0 mass% in terms of phosphorus atoms, and the obtained artificial leather was evaluated.
  • the results are shown in Table 2.
  • a grain-finished artificial leather was obtained in the same manner as in Example 1, except that the impregnation and the drying were performed with the solid content of the first phosphorous-based flame retardant particles changed to 40 mass%, to change the content of the first phosphorous-based flame retardant particles to 7.8 mass% in terms of phosphorus atoms, and the obtained artificial leather was evaluated.
  • the results are shown in Table 2.
  • a grain-finished artificial leather was obtained in the same manner as in Example 1, except that the content of the second phosphorous-based flame retardant particles blended in the surface resin layer was changed to 30 mass%, and the content of the first metal hydroxide to 8 mass%, to change a total content, in terms of phosphorus atoms and in terms of hydroxyl groups, to 8.6 mass%, and the obtained artificial leather was evaluated.
  • the results are shown in Table 2.
  • a grain-finished artificial leather was obtained in the same manner as in Example 6, except that the content of the first phosphorous-based flame retardant particles was changed to 1.5 mass% in terms of phosphorus atoms, and the obtained artificial leather was evaluated. The results are shown in Table 2.
  • a grain-finished artificial leather was obtained in the same manner as in Example 7, except that the content of the first phosphorous-based flame retardant particles was changed to 1.5 mass% in terms of phosphorus atoms, and the obtained artificial leather was evaluated. The results are shown in Table 2.
  • each of the artificial leather base materials obtained in Examples 1 to 7 had a bending resistance of 3.6 mm or more, and had a flexible texture, as well as favorable fullness and fold creases. Moreover, the self-extinguishing properties were favorable, and the smoke generation and the burn heat value were low, and, therefore, grain-finished artificial leathers with a high level of flame retardancy were obtained. On the other hand, the grain-finished artificial leather obtained in Comparative example 1, in which the amount of the first elastic polymer was small, had insufficient fullness, and also formed poor fold creases.
  • the grain-finished artificial leather obtained in Comparative example 2 in which the amount of the first elastic polymer was large, had a poor texture, and also had insufficient self-extinguishing properties, high smoke generation, a high burn heat value, and hence a low flame retardancy.
  • the grain-finished artificial leather of Comparative example 3 in which the average particle size of the flame retardant particles was large, showed variations in the burn test, and had insufficient self-extinguishing properties.
  • the grain-finished artificial leather of Comparative example 5 in which the amount of the first phosphorous-based flame retardant particles included in the artificial leather base material was large, had a reduced bending resistance, and thus had a hard texture.
  • the grain-finished artificial leather of Comparative example 6 in which the amount of the flame retardant particles in the resin layer was large, had a reduced bending resistance, thus had a hard texture, and also formed poor fold creases.
  • a grain-finished artificial leather according to the present invention can be preferably used in applications for which a high level of flame retardancy is required, including, for example, the interior materials and the seats in public transports such as aircrafts, vessels, and railroad, the interior materials and the seats in public buildings such as hotels and department stores, and also the interior materials in applications for shoes, clothing, gloves, bags, balls, interior decorations, and vehicle interior parts.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
EP17796022.6A 2016-05-09 2017-04-28 Grained artificial leather Active EP3456875B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2016093628 2016-05-09
PCT/JP2017/016956 WO2017195661A1 (ja) 2016-05-09 2017-04-28 銀付調人工皮革

Publications (3)

Publication Number Publication Date
EP3456875A1 EP3456875A1 (en) 2019-03-20
EP3456875A4 EP3456875A4 (en) 2020-01-01
EP3456875B1 true EP3456875B1 (en) 2022-03-02

Family

ID=60267209

Family Applications (1)

Application Number Title Priority Date Filing Date
EP17796022.6A Active EP3456875B1 (en) 2016-05-09 2017-04-28 Grained artificial leather

Country Status (7)

Country Link
US (1) US11015288B2 (ja)
EP (1) EP3456875B1 (ja)
JP (1) JP7029390B2 (ja)
KR (1) KR102372954B1 (ja)
CN (1) CN109072543B (ja)
TW (1) TWI726097B (ja)
WO (1) WO2017195661A1 (ja)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6860785B2 (ja) 2017-03-03 2021-04-21 テイ・エス テック株式会社 乗物用シート
JP7012080B2 (ja) * 2017-05-31 2022-01-27 株式会社クラレ 銀付調人工皮革及び銀付調人工皮革の製造方法
JP7455072B2 (ja) * 2018-12-03 2024-03-25 株式会社クラレ 立毛調人工皮革
WO2020137346A1 (ja) * 2018-12-28 2020-07-02 株式会社クラレ 立毛人工皮革及びコンポジット材
JP7265354B2 (ja) * 2018-12-28 2023-04-26 株式会社クラレ 立毛人工皮革及びそれを用いたコンポジット材
JP7265355B2 (ja) * 2018-12-28 2023-04-26 株式会社クラレ 立毛人工皮革及びコンポジット材
JP2020122252A (ja) * 2019-01-30 2020-08-13 アキレス株式会社 合成皮革
CN111074536A (zh) * 2019-12-25 2020-04-28 江苏领瑞新材料科技有限公司 一种耐火阻燃聚乙烯纤维ud布的制备方法
EP4083314A4 (en) * 2019-12-26 2024-01-10 Kuraray Co., Ltd. FULL GRAIN LEATHER TYPE SHEET

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3142100B2 (ja) * 1993-12-01 2001-03-07 株式会社クラレ シート状物及びその製造方法
JP2002294571A (ja) 2001-03-30 2002-10-09 Kuraray Co Ltd 難燃性皮革様シート基体およびその製造方法
JP4615138B2 (ja) 2001-03-27 2011-01-19 アキレス株式会社 皮革状シート物
EP1749920A4 (en) 2004-04-28 2009-07-22 Kuraray Co ART LEATHER WITH SILVERED TONE
GB0500629D0 (en) * 2005-01-13 2005-02-23 Dartex Coatings Ltd Fire retardance
JP4664135B2 (ja) * 2005-07-08 2011-04-06 大京化学株式会社 難燃性に優れたスエード調人工皮革およびその製造方法
JP4870412B2 (ja) 2005-10-31 2012-02-08 小松精練株式会社 繊維・ウレタン樹脂積層物およびその製造方法
JP4989522B2 (ja) 2008-03-05 2012-08-01 セーレン株式会社 難燃性合成皮革
CN102359023B (zh) * 2011-08-15 2014-02-05 浙江科一合成革有限公司 超纤环保阻燃合成革及其制备方法
US20160002846A1 (en) 2013-02-27 2016-01-07 Kuraray Co., Ltd. Artificial leather substrate, grain-like-finish artificial leather, method for producing artificial leather substrate, and modifying agent for artificial leather substrate
WO2014208685A1 (ja) 2013-06-27 2014-12-31 東洋紡株式会社 合成皮革
JP2016044375A (ja) * 2014-08-25 2016-04-04 株式会社クラレ 難燃性人工皮革基材、難燃性銀付調人工皮革及び難燃性銀付調人工皮革の製造方法

Also Published As

Publication number Publication date
WO2017195661A1 (ja) 2017-11-16
JPWO2017195661A1 (ja) 2019-04-04
EP3456875A1 (en) 2019-03-20
KR102372954B1 (ko) 2022-03-10
TW201809400A (zh) 2018-03-16
CN109072543B (zh) 2021-09-03
KR20190003627A (ko) 2019-01-09
US20190153666A1 (en) 2019-05-23
EP3456875A4 (en) 2020-01-01
US11015288B2 (en) 2021-05-25
JP7029390B2 (ja) 2022-03-03
TWI726097B (zh) 2021-05-01
CN109072543A (zh) 2018-12-21

Similar Documents

Publication Publication Date Title
EP3456875B1 (en) Grained artificial leather
WO2007007660A1 (ja) 難燃性に優れたスエード調人工皮革およびその製造方法
WO2016052189A1 (ja) シート状物の製造方法
JP2014074247A (ja) 銀付調人工皮革
JP2014034752A (ja) 伸縮性難燃人工皮革
JP2021021172A (ja) シート状物およびその製造方法
JP4708262B2 (ja) 難燃性立毛調人工皮革
WO2020203356A1 (ja) シート状物およびその製造方法
JP7265354B2 (ja) 立毛人工皮革及びそれを用いたコンポジット材
JP7148502B2 (ja) 人工皮革基材及び銀付調人工皮革
US11499266B2 (en) Grained artificial leather and method for manufacturing grained artificial leather
CN113260760B (zh) 立毛人造革及复合材料
JP2022101943A (ja) 人工皮革
JP2012017541A (ja) 銀付調人工皮革
JP7265355B2 (ja) 立毛人工皮革及びコンポジット材
WO2022097579A1 (ja) 立毛人工皮革
JP2007119936A (ja) 皮革様シート状物用基材およびその製造方法
JP2004360123A (ja) 難燃性皮革様シート基体およびその製造方法

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20181112

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
A4 Supplementary search report drawn up and despatched

Effective date: 20191202

RIC1 Information provided on ipc code assigned before grant

Ipc: D06M 101/32 20060101ALI20191126BHEP

Ipc: D06M 11/44 20060101ALI20191126BHEP

Ipc: D06M 13/282 20060101ALI20191126BHEP

Ipc: D06N 3/00 20060101AFI20191126BHEP

Ipc: D06M 13/224 20060101ALI20191126BHEP

Ipc: D06M 13/285 20060101ALI20191126BHEP

Ipc: D06M 13/288 20060101ALI20191126BHEP

Ipc: D06N 3/14 20060101ALI20191126BHEP

Ipc: D06M 11/45 20060101ALI20191126BHEP

Ipc: D06M 23/08 20060101ALI20191126BHEP

RIC1 Information provided on ipc code assigned before grant

Ipc: D06N 3/00 20060101AFI20201022BHEP

Ipc: D06M 13/288 20060101ALI20201022BHEP

Ipc: D06M 11/45 20060101ALI20201022BHEP

Ipc: D06N 3/14 20060101ALI20201022BHEP

Ipc: D06M 13/282 20060101ALI20201022BHEP

Ipc: D06M 11/44 20060101ALI20201022BHEP

Ipc: D06M 101/32 20060101ALI20201022BHEP

Ipc: D06M 23/08 20060101ALI20201022BHEP

Ipc: D06M 13/224 20060101ALI20201022BHEP

Ipc: D06M 13/285 20060101ALI20201022BHEP

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20210120

GRAJ Information related to disapproval of communication of intention to grant by the applicant or resumption of examination proceedings by the epo deleted

Free format text: ORIGINAL CODE: EPIDOSDIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

INTC Intention to grant announced (deleted)
GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20211124

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: AT

Ref legal event code: REF

Ref document number: 1472316

Country of ref document: AT

Kind code of ref document: T

Effective date: 20220315

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602017054107

Country of ref document: DE

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20220302

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220602

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220602

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1472316

Country of ref document: AT

Kind code of ref document: T

Effective date: 20220302

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220603

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220704

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220702

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602017054107

Country of ref document: DE

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20220430

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220428

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220430

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220430

26N No opposition filed

Effective date: 20221205

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220430

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220428

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230529

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20170428

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20240307

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20240313

Year of fee payment: 8

Ref country code: FR

Payment date: 20240308

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20240306

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220302